Clinical Genetics · 1980 · 35 citations · 17 references
MedicineGeneticsMolecular GeneticsCytogeneticsHuman GeneticsMedical GeneticsAdrenal Disorder GeneticsAdrenal DisordersCongenital Endocrine DisordersGenetic DisordersInherited Endocrine SyndromesNeurogenetic DisordersX-linked Adrenoleukodystrophy
Cerebral sclerosis and Addison disease were observed at age 14 years in a previously healthy sister of an affected boy. Clinical findings and family history established the diagnosis of X-linked adrenoleukodystrophy, which is normallly confined to males. The affected female has a normal karyotype; both X chromosomes are morphologically inconspicuous. Thus, this patient may be the first documented example of clinically manifest adrenoleukodystrophy in a heterozygote, which supports our previous conclusion that this X-linked locus is subject to inactivation.
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Gene Action in the X-chromosome of the Mouse (Mus musculus L.)
Mary F. Lyon · Nature · 1961 · 4K citations
The rate of spontaneous mutation of a human gene
J. B. S. Haldane · Journal of Genetics · 1935 · 524 citations
Herbert H. Schaumburg, James M. Powers, CEDRICS RAINE et al. · Neurology · 1977 · 168 citations
Medicine, Endocrinology, Neurology +17
T. Mohandas, L J Shapiro, R S Sparkes et al. · Proceedings of the National Academy of Sciences · 1979 · 154 citations · Full text